Canonical Allele Identifier: CA399310429

Gene: ERBB2

Linked Data

• dbSNP Id: rs1038581447
• MyVariant Identifiers: chr17:g.37883623G>T (hg19) ; chr17:g.39727370G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727370G>T , CM000679.2:g.39727370G>T	GRCh38
NC_000017.10:g.37883623G>T , CM000679.1:g.37883623G>T	GRCh37
NC_000017.9:g.35137149G>T	NCBI36
NG_007503.1:g.44231G>T , LRG_724:g.44231G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3235G>T MANE Select	ENSP00000269571.4:p.Glu1079Ter
ENST00000269571.9:c.3235G>T	ENSP00000269571.4:p.Glu1079Ter
ENST00000406381.6:c.3145G>T	ENSP00000385185.2:p.Glu1049Ter
ENST00000445658.6:c.2407G>T	ENSP00000404047.2:p.Glu803Ter
ENST00000541774.5:c.3190G>T	ENSP00000446466.1:p.Glu1064Ter
ENST00000578373.5:c.*3025G>T	ENSP00000463427.1:n.*3025G>T
ENST00000584450.5:c.3160-319G>T	ENSP00000463714.1:n.3160-319G>T
ENST00000584601.5:c.3145G>T	ENSP00000462438.1:p.Glu1049Ter
NM_001005862.2:c.3145G>T , LRG_724t1:c.3145G>T	NP_001005862.1:p.Glu1049Ter
NM_001289936.1:c.3190G>T , LRG_724t4:c.3190G>T	NP_001276865.1:p.Glu1064Ter
NM_001289937.1:c.3160-319G>T	NP_001276866.1:n.3160-319G>T
NM_004448.3:c.3235G>T , LRG_724t2:c.3235G>T	NP_004439.2:p.Glu1079Ter
NR_110535.1:n.3559G>T
XM_024450641.1:c.3373G>T	XP_024306409.1:p.Glu1125Ter
XM_024450642.1:c.3328G>T	XP_024306410.1:p.Glu1110Ter
XM_024450643.1:c.3283G>T	XP_024306411.1:p.Glu1095Ter
NM_001005862.3:c.3145G>T	NP_001005862.1:p.Glu1049Ter
NM_001289936.2:c.3190G>T	NP_001276865.1:p.Glu1064Ter
NM_001289937.2:c.3160-319G>T	NP_001276866.1:n.3160-319G>T
NM_001382782.1:c.3145G>T	NP_001369711.1:p.Glu1049Ter
NM_001382783.1:c.3145G>T	NP_001369712.1:p.Glu1049Ter
NM_001382784.1:c.3352G>T	NP_001369713.1:p.Glu1118Ter
NM_001382785.1:c.3337G>T	NP_001369714.1:p.Glu1113Ter
NM_001382786.1:c.3316G>T	NP_001369715.1:p.Glu1106Ter
NM_001382787.1:c.3310G>T	NP_001369716.1:p.Glu1104Ter
NM_001382788.1:c.3265G>T	NP_001369717.1:p.Glu1089Ter
NM_001382789.1:c.3256G>T	NP_001369718.1:p.Glu1086Ter
NM_001382790.1:c.3232G>T	NP_001369719.1:p.Glu1078Ter
NM_001382791.1:c.3226G>T	NP_001369720.1:p.Glu1076Ter
NM_001382792.1:c.3199G>T	NP_001369721.1:p.Glu1067Ter
NM_001382793.1:c.3193G>T	NP_001369722.1:p.Glu1065Ter
NM_001382794.1:c.3193G>T	NP_001369723.1:p.Glu1065Ter
NM_001382795.1:c.3187G>T	NP_001369724.1:p.Glu1063Ter
NM_001382796.1:c.3148G>T	NP_001369725.1:p.Glu1050Ter
NM_001382797.1:c.3136G>T	NP_001369726.1:p.Glu1046Ter
NM_001382798.1:c.3079G>T	NP_001369727.1:p.Glu1027Ter
NM_001382799.1:c.3055G>T	NP_001369728.1:p.Glu1019Ter
NM_001382800.1:c.3049G>T	NP_001369729.1:p.Glu1017Ter
NM_001382801.1:c.3031G>T	NP_001369730.1:p.Glu1011Ter
NM_001382802.1:c.2977G>T	NP_001369731.1:p.Glu993Ter
NM_001382803.1:c.3118-319G>T	NP_001369732.1:n.3118-319G>T
NM_001382804.1:c.2407G>T	NP_001369733.1:p.Glu803Ter
NM_001382805.1:c.2284G>T	NP_001369734.1:p.Glu762Ter
NM_001382806.1:c.2197G>T	NP_001369735.1:p.Glu733Ter
NM_004448.4:c.3235G>T MANE Select	NP_004439.2:p.Glu1079Ter
NR_110535.2:n.3473G>T